Priovoulos Nikos, Andersen Mads, Dumoulin Serge O, Boer Vincent O, van der Zwaag Wietske
From the Spinoza Centre for Neuroimaging, Royal Netherlands Academy of Arts and Sciences (KNAW), Meibergdreef 75, 1105 BK Amsterdam, the Netherlands (N.P., S.O.D., W.v.d.Z.); Computational Cognitive Neuroscience and Neuroimaging, Netherlands Institute for Neuroscience, Amsterdam, the Netherlands (N.P., S.O.D., W.v.d.Z.); Philips Healthcare, Copenhagen, Denmark (M.A.); Lund University Bioimaging Centre, Lund University, Lund, Sweden (M.A.); Department of Experimental and Applied Psychology, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands (S.O.D.); Department of Experimental Psychology, Utrecht University, Utrecht, the Netherlands (S.O.D.); and Danish Research Centre for Magnetic Resonance, Centre for Functional and Diagnostic Imaging and Research, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark (V.O.B.).
Radiology. 2023 Apr;307(2):e220989. doi: 10.1148/radiol.220989. Epub 2023 Jan 17.
Background The human cerebellum has a large, highly folded cortical sheet. Its visualization is important for various disorders, including multiple sclerosis and spinocerebellar ataxias. The derivation of the cerebellar cortical surface in vivo is impeded by its high foliation. Purpose To image the cerebellar cortex, including its foliations and lamination, in less than 20 minutes, reconstruct the cerebellocortical surface, and extract cortical measures with use of motion-corrected, high-spatial-resolution 7.0-T MRI. Materials and Methods In this prospective study, conducted between February 2021 and July 2022, healthy participants underwent an examination with either a 0.19 × 0.19 × 0.5-mm, motion-corrected fast low-angle shot (FLASH) sequence (14.5 minutes) or a whole-cerebellum 0.4 × 0.4 × 0.4-mm, motion-corrected magnetization-prepared 2 rapid gradient-echo (MP2RAGE) sequence (18.5 minutes) at 7.0 T. Four participants underwent an additional FLASH sequence without motion correction. FLASH and MP2RAGE sequences were used to visualize the cerebellar cortical layers, derive cerebellar gray and white matter segmentations, and examine their fidelity. Quantitative measures were compared using repeated-measures analyses of variance or paired tests. Results Nine participants (median age, 36 years [IQR, 25-42 years; range, 21-62 years]; five women) underwent examination with the FLASH sequence. Nine participants (median age, 37 years [IQR, 34-42 years; range, 25-62 years]; five men) underwent examination with the MP2RAGE sequence. A susceptibility difference between the expected location of the granular and molecular cerebellar layers was visually detected in the FLASH data in all participants. The segmentations derived from the whole-cerebellum MP2RAGE sequence showed the characteristic anatomic features of the cerebellum, like the transverse fissures and splitting folds. The cortical surface area (median, 949 cm [IQR, 825-1021 cm]) was 1.8 times larger, and the cortical thickness (median, 0.88 mm [IQR, 0.81-0.93 mm]) was five times thinner than previous in vivo estimates and closer to ex vivo reference data. Conclusion In vivo imaging of the cerebellar cortical layers and surface and derivation of quantitative measures was feasible in a clinically acceptable acquisition time with use of motion-corrected 7.0-T MRI. Published under a CC BY 4.0 license. See also the editorial by Dietrich in this issue.
人类小脑有一个大的、高度折叠的皮质层。其可视化对于包括多发性硬化症和脊髓小脑共济失调在内的各种疾病很重要。小脑皮质表面在体内的推导因其高度叶状化而受阻。目的:在不到20分钟的时间内对小脑皮质进行成像,包括其叶状结构和分层,重建小脑皮质表面,并使用运动校正的高空间分辨率7.0-T MRI提取皮质测量值。材料和方法:在2021年2月至2022年7月进行的这项前瞻性研究中,健康参与者在7.0 T下接受了0.19×0.19×0.5-mm的运动校正快速低角度激发(FLASH)序列(14.5分钟)或全小脑0.4×0.4×0.4-mm的运动校正磁化准备快速梯度回波(MP2RAGE)序列(18.5分钟)检查。四名参与者额外接受了未进行运动校正的FLASH序列检查。FLASH和MP2RAGE序列用于可视化小脑皮质层,推导小脑灰质和白质分割,并检查其保真度。使用重复测量方差分析或配对检验比较定量测量值。结果:九名参与者(中位年龄36岁[四分位间距,25 - 42岁;范围,21 - 62岁];五名女性)接受了FLASH序列检查。九名参与者(中位年龄37岁[四分位间距,34 - 42岁;范围,25 - 62岁];五名男性)接受了MP2RAGE序列检查。在所有参与者的FLASH数据中,肉眼可检测到颗粒层和分子层预期位置之间的磁化率差异。从全小脑MP2RAGE序列得出的分割显示了小脑的特征性解剖特征,如横裂和分裂褶皱。皮质表面积(中位数,949平方厘米[四分位间距,825 - 1021平方厘米])比先前的体内估计值大1.8倍,皮质厚度(中位数,0.88毫米[四分位间距,0.81 - 0.93毫米])比先前的体内估计值薄五倍,且更接近体外参考数据。结论:使用运动校正的7.0-T MRI,在临床可接受的采集时间内对小脑皮质层和表面进行体内成像并推导定量测量值是可行的。根据知识共享署名4.0许可发布。另见本期Dietrich的社论。